510(k) Report

FDA applicant

Dental Products of USA, Inc.

Miami, FL1 decision2004–20040 recalls

FDA records 1 decision for Dental Products of USA, Inc. (Miami, FL) in 2004: 1 510(k) clearance. All are in product code EBZ (Activator, Ultraviolet, For Polymerization). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Dental Products of USA, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dental Products of USA, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dental Products of USA, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Dental Products of USA, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report